Manufacturing Associate I

Published
October 8, 2020
Location
Fremont, CA
Category
Job Type

Description

11353328
Manufacturing Associate I 

Responsibilities:

  • Prepare a variety of media and stock solutions that are transferred from tank to bag or tank to tank in order to support cell culture main operations to facilitate proper cellular growth per SOP.
  • Able to follow SOP’s to perform routine cleaning activities of parts and equipment using manual cleaning methods, designated parts washers, Clean-In-Place (CIP) and COP(Clean-Out-Of-Place) systems. As well as collecting rinse water samples and performing swabs on required equipment for testing.
  • Execute proper documentation and measures to initiate changing over of parts and equipment to be released for use.
  • Performs a majority of operations in a cGMP clean room environment.
  • Practices ergonomic safety and use appropriate personal protective equipment (PPE) in all operations.
  • Documents execution of operations through the Bio Manufacturing Execution System (BioMES), batch record and equipment use logbook using Good Documentation Practices (GDP). Interchanging between electronic and paper documentation procedures.
  • Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.
  • Reports any issues related to manufacturing performance, process and safety to the team lead or Manager in order to ensure safety and compliance with regulations and cGMPs and to facilitate continuous process improvement.
  • Participates in training and development opportunities in order to gain an understanding of SOPs,
  • Performs routine housekeeping of the manufacturing plant using the 5S organization methodology by using appropriate equipment safety signage, labeling of parts-in-process, sweeping water pools to the floor drain, and picking up parts from the floor.
  • Collaborates within team and department in order to follow best practices and meet department goals.

 Qualifications:

  • Experience working with established GMP procedures and bulk manufacturing. Technical knowledge of manufacturing systems, methods and procedures.
  • Understanding of cell culture processes. Possess effective troubleshooting skills with equipment and/or process.
  • Demonstrated ability to be organized and work well in small work groups.
  • Must be able to assist in trouble shooting activities and repairs to production equipment under the guidance of more experienced technicians.
  • Demonstrated mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions.
  • Detail oriented. Demonstrated ability to read, comprehend, and follow written instructions.
  • Demonstrated written and verbal communication skills are required.
  • Must be able to work in a team environment.
  • Experiences in related biotechnology/pharmaceutical industry strongly preferred
  • Must be able to learn and perform basic computer operations such as MS Office and Outlook and other computer based software
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